EP0686690A1 - Gear and transmission lubricant compositions of improved sludge-dispersibility, fluids comprising the same - Google Patents

Gear and transmission lubricant compositions of improved sludge-dispersibility, fluids comprising the same Download PDF

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Publication number
EP0686690A1
EP0686690A1 EP94304031A EP94304031A EP0686690A1 EP 0686690 A1 EP0686690 A1 EP 0686690A1 EP 94304031 A EP94304031 A EP 94304031A EP 94304031 A EP94304031 A EP 94304031A EP 0686690 A1 EP0686690 A1 EP 0686690A1
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alkyl
monomer
composition according
esters
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German (de)
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EP0686690B1 (en
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Shoji Takigawa
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Sanyo Chemical Industries Ltd
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Sanyo Chemical Industries Ltd
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M161/00Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/08Ammonium or amine salts
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/10Thio derivatives
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    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/12Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having a phosphorus-to-carbon bond
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    • C10M149/00Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
    • C10M149/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M149/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
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    • C10M149/00Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
    • C10M149/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M149/10Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
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    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • C10M159/20Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
    • C10M159/24Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
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    • C10M167/00Lubricating compositions characterised by the additive being a mixture of a macromolecular compound, a non-macromolecular compound and a compound of unknown or incompletely defined constitution, each of these compounds being essential
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    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/02Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/022Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
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    • C10M2217/02Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/022Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
    • C10M2217/023Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group the amino group containing an ester bond
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    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/02Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/028Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
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    • C10M2217/06Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046Overbasedsulfonic acid salts
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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    • C10M2223/04Phosphate esters
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/041Triaryl phosphates
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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    • C10M2223/042Metal salts thereof
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    • C10M2223/049Phosphite
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
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    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/042Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
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    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/044Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
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    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/046Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives

Abstract

A gear or transmission lubricant composition, comprising a major portion of mineral base oil, containing added thereto (A) a phosphorus-containing metal-free organic compound, such as a phosphate ester or amine salt thereof, and (B) an oil-soluble copolymer of (a) an alkyl (meth)acrylate and (b) a N,N-dialkylaminoalkyl (meth)acrylate, shows improved sludge dispersibility, and is useful as automatic transmission fluid.

Description

    BACKGROUND OF THE INVENTION 1. Field of the Invention:
  • This invention relates to gear and transmission lubricant compositions, having improved sludge-dispersibility, particularly, those useful for automotive gear and transmission fluids.
  • 2. Description of the Prior Art:
  • Heretofore, in order to improve anti-wear or lubricating qualities and sludge-dispersibility, required for automotive gear and transmission fluids, there have been known those containing added thereto anti-wear or lubricating agents comprising phosphorus-containing organic compound, such as phosphate or phosphite esters or amine salts thereof, together with lower molecular weight dispersants, such as succinimides and benzyl amine. For example, US Patent 4,800,029 discloses an aotomatic transmission fluid (ATF) comprising a solvent-purified 150 neutral oil, containing added thereto an oleamide phosphate as anti-wear agent and polybutenyl succinimide as dispersant.
  • These fluids containing added thereto phosphorus-containing organic compounds together with lower molecular weight dispersants, however, have drawbacks, such that dispersabilities become insufficient under severe service conditions likely to form larger sludge, encounterd with friction or wear, accompanied with recent tendency of miniturization and output power up of automobiles; and it is desired to improve the dispersibility.
  • SUMMARY OF THE INVENTION
  • It is an object of the present invention to provide a gear or transmission lubricant composition having improved sludge-dispersibility.
  • It is another object of this invention to provide a gear or transmission lubricant composition capable of providing reduced sludge formation.
  • It is still another object of the invention to provide a gear or transmission lubricant composition capable of maintaining good sludge-dispersibility even at severe service conditions.
  • It is yet another object of the invention to provide a gear oil or a transmission fluid, particularly ATF, having improved sludge-dispersibility.
  • Briefly, these and other objects of the present In vention as hereinafter will become more readily apparent have been attained broadly by a gear or transmission lubricant composition, which comprises a major portion of mineral base oil, containing added thereto a minor proportion of (A) at least one phosphorus-containing metal-free organic compound and (B) at least one oil-soluble copolymer containing 92∼99 % by weight of monomer unis of (a) alkyl (meth)acrylate and 1∼8 % by weight of monomer unis of (b) N,N-dialkylaminoalkyl (meth)acrylate.
  • [In the above and hereinafter, (meth)acrylate represents acrylate and/or methacrylate; and similar expressions are used hereinafter].
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Base Oil
  • Suitable base oils used in the present invention include mineral oils, having a viscosity of usually 1∼50 cSt (centistokes), preferably 2∼30 cSt at 100°C. Base oils having a viscosity higher than 50 cSt give rise to energy loss because of too high viscosity resistance. Oils of less than 1 cSt are liable to result in evaporation during use at elevated temperature and to cause seizing on account of shortage of oil film exposed to extreme pressure at lubricationg parts. Viscosity index (hereinafter referred to as VI) of base oils is generally at least 60, preferably at least 70. Oils of VI less than 60 do not provide satisfactory viscosity-temperature properties. Illustrative of suitable base oils are 100 neutral oil, 150 neutral oil, 300 neutral oil, 500 neutral oil, 150 bright stoch and the like.
  • (A) Phosphorus-containing Organic Compound
  • Suitable phosphorus-containing metal-free organic compound (A) include phosphate esters, phosphite esters, phosphonate esters, and amine salts of these esters; as well as mixtures of two or more of these compounds.
  • Examples of these compounds include ones represented by any of the following formulae (1), (2), (3) and (4).



            O=P(OR)p(OH)3-p   (1)





            O=P(OR)q(OH)3-q · NHrR' 3-r   (2)





            P(OR)p(OH)3-p   (3)





            P(OR)q(OH)3-q · NHrR' 3-r   (4)



       In the formulae (1), (2), (3) and (4), p is an integer of 1, 2 or 3; q and r are independently integers of 1 or 2.
  • R and R' are independently selected from the group consisting of saturated or unsaturated alkyl groups containing at least 4 carbon atoms, aryl groups and alkyl-subsituted aryl groups. Examples of R and R' include straight-chain or branched, saturated or unsaturated alkyl groups (aliphatic hydrocarbyl groups) containing 4∼30 or more, preferably 4∼20 carbon atoms, such as n-, iso-, sec- and t-butyl, hexyl, octyl, 2-ethylhexyl, decyl, dodecyl, tridecyl, tetradecyl, hexadecyl, octadecyl, eicocyl, and oleyl groups; aryl groups, such as phenyl and naphthyl groups; and aryl groups subsituted substituted with one or more alkyl groups containing 1∼20, preferably 1∼10 carbon atoms in the alkyl group, such as tolyl group. These alkyl, aryl and alkyl-subsituted aryl groups may be ether group-containing ones, such as lauroxyethyl, lauroxypropyl, oleoxyethyl groups.
  • Illustrative examples of these compounds of the following formulae (1), (2), (3) and (4) are as follows:
    • (1) mono-, di- and tri-alkyl and/or aryl phospates, such as mono-oleyl phosphate, tricrezyl phosphate, and dibutyl lauroxypropyl phosphate;
    • (2) salts of mono- or di-alkyl and/or aryl phospates as above, with mono- or di-alkyl amine, such as di-2-ethylhexyl amine;
    • (3) mono-, di- and tri-alkyl and/or aryl phospites, such as di-n-butyl phospite, tributyl phospite,
    • (4) salts of mono- or di-alkyl and/or aryl phospites as above, with mono- or di-alkyl amine, such as di-2-ethylhexyl amine.
  • Phosphorus-containing compounds, as written in C.J.Boner "Gear and Transmission Lubricants" (1964 Reinhold Publishing Corp.), page 94, Table 3.8, may also be used.
  • Among these phosphorus-containing metal-free organic compound (A), preferred are those of the formula (1), particularly alkyl phosphate containing 4∼18 carbon atoms in the alkyl group. The most preferred is mono-oleyl phosphate.
  • The amount of the phosphorus-containing metal-free organic compound (A), usually 0.01∼5 %, preferably 0.1∼3 %, based on the weight of the lubricant composition.
  • (B) Oil-soluble Copolymer
  • Suitable alkyl (meth)acrylates (a), constituting said oil-soluble copolymer (B), are ones contains 1∼24 carbon atoms in the alkyl group; and include, for example: (a₁) C8∼20 alkyl (meth)acrylates, such as octyl, decyl, dodecyl, tridecyl, tetradecyl, hexadecyl, octadecyl and eicocyl (meth)acrylates; (a₂) C1∼4 alkyl (meth)acrylates, such as methyl, ethyl, propyl and butyl (meth)acrylates; (a₃) C5∼7 alkyl (meth)acrylates, such as pentyl, hexyl and heptyl (meth)acrylates; (a₄) C21∼24 alkyl (meth)acrylates, such as Nafol 20+ and Nafol 22+ (produced by Kondea-Chemie; and combinations of two or more of them.
  • Among these, preferred are (a₁) (particularly decyl methacrylate and dodecyl methacrylate), and combinations thereof with (a₂) (particularly methyl methacrylate).
  • Suitable N,N-dialkylaminoalkyl (meth)acrylate (b), constituting said oil-soluble copolymer (B), include one by the following formula (5):
    Figure imgb0001

    wherein R₁ and R₂ are the same or different alkyl groups containing not more than 10 carbon atoms, R₃ is an alkylene group containing 2∼10 carbon atoms, and R₄ is hydrogen atom or methyl group.
  • Illustrative of (b) are N,N-dimethylaminoethyl (meth)acrylates, N,N-diethylaminoethyl (meth)acrylates, N,N-diethylaminohexyl (meth)acrylates, N,N-dimethylaminopropyl (meth)acrylates, N,N-dibutylaminooctyl (meth)acrylates, and mixtures of two or more of them. Among these, preferred are N,N-dimethylaminoethyl methacrylate and N,N-diethylaminoethyl methacrylate.
  • Said oil-soluble copolymer (B) may contain monomer unis of (c) one or more of N-vinyl-pyrrolidone and morpholinoalkyl (meth)acrylates, to improve sludge dispersibility. Suitable morpholinoalkyl (meth)acrylates include ones containing 2∼4 or more carbon atoms in the alkylene, such as morpholinoethyl and morpholinopropyl (meth)acrylates. Among these, preferred is N-vinylpyrrolidone.
  • Said copolymer (B) may further contain monomer unis of (d) one or more additional monomers. Exemplery of additional monomers (d) are aromatic vinyl compounds, such as styrene and vinyltoluene; esters (such as alkyl esters containing not more than 20 carbon atoms in the alkyl group) of unsaturated dicarboxylic acid (such as maleic, fumaric and itaconic acids), for example, dibutyl, dioctyl and dilauryl maleates, and dihexyl, dihexadecyl and dioctadecyl fumarates; and vinyl esters (ones containing not more than 5 carbon atoms in the alkyl group), such as vinyl acetate and vinyl propionate; and so on. Among these, preferred is styrene, in view of VI and bodying effects.
  • The contents of these monomers unis of (a), (b), (c) and (d) in said oil-solubult copolymer (B) are as follows:
    Usually preferably
    (a) 92∼99 % 94∼98 %
    (a₁) 52∼99 % 64∼93 %
    (a₂) 0∼40 % 5∼30 %
    (b) 1∼8 % 2∼6 %
    (c) 0∼10 % ∼ %
    (d) 0∼30 % 0∼20 %
  • In the above and hereinafter, % represents % by weight.
  • Copolymer (B) can be produced by usual polymerization thechniques, for instance, by radical polymerization of (a) and (b) with or without (c) and/or (d), within a solvent, such as mineral oil. There may be used any polymerization catalysts, for example, azo compounds, such as azobis-isobutyrenitrile (hereinafter referred to as AIBN) and azobisvaleronitrile, and peroxides, such as benzoyl peroxide, cumyl peroxide and lauryl peroxide, with or without chain transfer agents, such as mercaptans (lauryl mercaptan and the like).
  • Said copolymer (B) is oil-soluble and is effective as a VI improver in addition to dispersant. To attain these effects, (B) has a weight-average molecular weight (hereinafter referred to as Mw ¯
    Figure imgb0002
    ), as measured by GPC (gel permeation chromatography) using calibration curve of polystyrene, of generally 20,000∼200,000, preferably 30,000∼150,000. Polymer of too high molecualr weight causes degradation to form shorter chain polymer when subjected to shearing and cannot maintain necessary viscosity and VI for a long period of time. Polymer of too low molecular weight is to be used in a larger amount in order to attain sufficient viscosity.
  • The gear or transmission lubricant composition of the present invention, usually contains, as a practical use level of the lubricant, 0.01∼5 %, preferably 0.05∼3 %, more preferably 0.1∼2 % of said phosphorus-containing organic compound (A) and 1∼30 %, preferably 2∼25 %, more preferably 3∼20 % of said oil-soluble copolymer (B).
  • Concentrate containing (A) and/or (B) in higher concentration than the above range may be prepared, and this is diluted to lebel of practical use.
  • The composition of this invention may further contains one or more additives, usually used in gear and transmission lubricants. Such additives include, for example, detergents, such as sulfonates, salicylates, phenates and naphthenates; dispersants, such as alkenylsuccinimides and Mannich condensates; anti-oxidants, such as thiophosphates, amines and hindered phenols; oiliness additives, such as fatty acids and esters thereof; antiwear agent, other than (A), such as molybdenum dithiophosphate and molybdenum carbamate; and extreme pressure agents, such as sulfur-containing compounds, phosphorus-containing compounds and chlorine-containing compounds. These additives can be used in such amounts : 0∼10 % of the detergent, 0∼10 % of the dispersant, 0∼5 % of the anti-oxidant, 0∼3 % of the oiliness additive, 0∼10 % of the antiwear agent, and 0∼10 % of the extreme pressure agent.
  • Compositions of the invention, containing said phosphorus-containing organic compound (A) and said oil-soluble copolymer (B), are useful as gear and transmission lubricants, particularly automotive gear lubricants. Excellent effects can be attained especially when used as automatic transmission fluid for torque converters.
  • Having generally described the invention, a more complete understanding can be obtained by reference to certain specific examples, which are included for purposes of illustration only and are not intended to be limiting unless otherwise specified.
  • In the following examples, parts represents parts by weight.
  • Preparation of Copolymers
  • Into a reaction vessel equipped with a stirrer, a thermometer and a condensor, 150 parts of a mineral oil (100 neutral oil) were charged and heated to 70°C under an atmosphere of nitrogen. Then, thereto were added dropwise the monomers (parts) written in Table 1 together with 1.7 parts of AIBN and 2.0 parts of lauryl mercaptan over 2 hours at the temperature, followed by heating to 100°C for 3 hours to complete the polymerization to obtain a solution of copolymer having Mw ¯
    Figure imgb0003
    as written in Table 1.
    Figure imgb0004
  • Examples 1 to 10, and Comparative Examples 1 to 6
  • According to the following Formulation I or II (%), mineral oil compositions were prepared.
    Formulation I II
    Each copolymer solution 10 18
    Oleyl amine salt of dilauryl phosphate 1 -
    Octyl amine salt of dioleyl phosphate - 1
    Polybutenylsuccinimide (Hitec E638*) 3 -
    Polyolefin sulfide (TLA369, produced by Texaco) - 5
    Perbasic calcium sulfonate (Hitec E611*) 1 1
    Dialkylzinc dithiophosphate (Amoco 194) 0.3 -
    Dialkylzinc dithiophosphate (Amoco 198) - 0.5
    2,6-di-tert-butyl-p-crezole (Lubrizol 817) 0.2 -
    A mineral oil (100 neutral) 84.5 74.5
    (Notes) *:produced by Ethyl Cooper.
  • Resistance to oxidation of each composition was evaluated in accordance with JIS K2514, measuring the amounts of sludge (pentane-insuluble matter, %) of Methods A and B. Method A represents the amount of sludge obtained by centrifuging the oil after the test, and Method B represents the amount of sludge obtained by centrifuging the oil to which a flocculant was added after the test. The amounts of Methds A and B show resistance to oxidation, and the difference between the amounts of Methds A and B means sludge dispersability.
  • The results were as shown in Table 2.
    Figure imgb0005
  • As apparent from Tables 1 and 2, compositions of the present invention provided extremely small amount of sludge and showed excellent sludge dispersibility and resistance to oxidation.
  • Compositions of this invention, when used as gear and transmission lubricants, particularly automatic transmission fluid for torque converters, can attain excellent sludge dispersibility with remarkably reducing sludge formation.

Claims (10)

  1. A gear or transmission lubricant composition, which comprises
    a major portion of mineral base oil, having a viscosity of 1∼50 cSt. at 100°C and having a viscosity index of at least 60; containing, based on the weight of the composition,
    0.01∼5 % of (A) at least one phosphorus-containing metal-free organic compound, selected from the group consisting of phosphate esters, phosphite esters, phosphonate esters, and amine salts of these esters;
    and 1∼30 % of (B) at least one oil-soluble copolymer containing 92∼99 %, preferably 94∼98 % by weight of monomer unis of (a) alkyl acrylate or methacrylate preferavly containing 1∼24 carbon atoms in the alkyl group, and 1∼8 %, preferably 2∼6 % by weight of monomer unis of (b) N,N-dlalkylaminoalkyl acrylate or methacrylate.
  2. A composition according to Claim 1, wherein (A) is selected from the group consisting of compounds represented by any of the following formulae (1), (2), (3) and (4):



            O=P(OR)p(OH)3-p   (1)





            O=P(OR)q(OH)3-q · NHrR' 3-r   (2)





            P(OR)p(OH)3-p   (3)





            P(OR)q(OH)3-q · NHrR' 3-r   (4)



    wherein p is an integer of 1∼3; q and r are independently integers of 1 or 2; R and R' are independently selected from the group consisting of saturated or unsaturated alkyl groups containing at least 4 carbon atoms, aryl groups and alkyl-subsituted aryl groups.
  3. A composition according to Claim 1 or 2, wherein the monomer (a) comprises (a₁) alkyl acrylate or methacrylate containing 8∼20 carbon atoms in the alkyl group, and optionally (a₂) alkyl acrylate or methacrylate containing 1∼4 carbon atoms in the alkyl group.
  4. A composition according to Claim 3, wherein said copolymer contains 52∼99 %, preferably 64∼93 % by weight of monomer unis of (a₁), and 0∼40 %, preferably 5∼30 % by weight of mononer unis of (a₂).
  5. A composition according to any one of Claims 1 to 4, wherein said copolymer further contains upto 10 % by weight of monomer unis of (c) at least one monomer selected from the group consisting of N-vinyl-pyrrolidone, morpholinoalkyl acrylate and morpholinoalkyl methacrylate; and/or upto 30 % by weight of monomer unis of (d) at least one monomer selected from the group consisting of aromatic vinyl compound, alkyl esters of unsaturated dicarboxylic acid containing not more than 20 carbon atoms in the alkyl group, and vinyl esters.
  6. A composition according to any one of Claims 1 to 5, wherein said copolymer has a weight-average molecular weight of 20,000∼200,000.
  7. A composition according to any one of Claims 1 to 6, which further contains one or more additives as follows:
    1) detergent preferably selected from sulfonates, salicylates, phenates and naphthenates;
    2) dispersant preferably selected from alkenylsuccinimides and Mannich condensates;
    3) anti-oxidant preferably selected from thiophosphates, amines and hindered phenols;
    4) oiliness additive preferably selected from fatty acids and esters thereof;
    5) antiwear agent preferably selected from molybdenum dithiophosphate and molybdenum carbamate; and
    6) extreme pressure agent preferably selected from sulfur-containing compounds, phosphorus-containing compounds and chlorine-containing compounds.
  8. A composition according to Claim 7, which contains said additive in such amounts as follows:
    1) 0∼10 % by weight of said detergent,
    2) 0∼10 % by weight of said dispersant,
    3) 0∼5 % by weight of said anti-oxidant,
    4) 0∼3 % by weight of said oiliness additive,
    5) 0∼10 % by weight of said antiwear agent, and
    6) 0∼10 % by weight of said extreme pressure agent.
  9. A gear oil, particularly an automatic transmission fluid, comprising the composition according to any one of Claims 1 to 8.
  10. A torque converter, contained therein the automatic transmission fluid according to Claim 9.
EP94304031A 1994-06-06 1994-06-06 Gear and transmission lubricant compositions of improved sludge-dispersibility. Revoked EP0686690B1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
DE69431710T DE69431710T2 (en) 1994-06-06 1994-06-06 Gear and power transmission lubricant compositions with improved slurry dispersing properties.
EP94304031A EP0686690B1 (en) 1994-06-06 1994-06-06 Gear and transmission lubricant compositions of improved sludge-dispersibility.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP94304031A EP0686690B1 (en) 1994-06-06 1994-06-06 Gear and transmission lubricant compositions of improved sludge-dispersibility.

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EP0686690A1 true EP0686690A1 (en) 1995-12-13
EP0686690B1 EP0686690B1 (en) 2002-11-13

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5807815A (en) * 1997-07-03 1998-09-15 Exxon Research And Engineering Company Automatic transmission fluid having low Brookfield viscosity and high shear stability
WO2003089554A1 (en) * 2002-04-15 2003-10-30 The Lubrizol Corporation Phosphorus salts of nitrogen containing copolymers and lubricants containing the same
DE102011076364A1 (en) 2011-05-24 2012-11-29 Evonik Rohmax Additives Gmbh Lubricant composition with phosphate-functionalized polymers
WO2020101969A1 (en) * 2018-11-12 2020-05-22 The Lubrizol Corporation Method of lubricating an automotive or industrial gear

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Publication number Priority date Publication date Assignee Title
US2892784A (en) * 1955-06-29 1959-06-30 California Research Corp Oxidation resistant lubricant compositions
US3309317A (en) * 1964-06-08 1967-03-14 Shell Oil Co Lubricating composition
US3640872A (en) * 1968-10-25 1972-02-08 Texaco Inc Automatic transmission fluid
US3702824A (en) * 1970-06-12 1972-11-14 Texaco Inc Friction reducing agent for lubricants
GB1413677A (en) * 1972-10-11 1975-11-12 Sun Oil Co Pennsylvania Lubricant composition
US4036768A (en) * 1976-06-14 1977-07-19 Texaco Inc. Polymethacrylate and lube composition thereof

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Publication number Priority date Publication date Assignee Title
US2892784A (en) * 1955-06-29 1959-06-30 California Research Corp Oxidation resistant lubricant compositions
US3309317A (en) * 1964-06-08 1967-03-14 Shell Oil Co Lubricating composition
US3640872A (en) * 1968-10-25 1972-02-08 Texaco Inc Automatic transmission fluid
US3702824A (en) * 1970-06-12 1972-11-14 Texaco Inc Friction reducing agent for lubricants
GB1413677A (en) * 1972-10-11 1975-11-12 Sun Oil Co Pennsylvania Lubricant composition
US4036768A (en) * 1976-06-14 1977-07-19 Texaco Inc. Polymethacrylate and lube composition thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5807815A (en) * 1997-07-03 1998-09-15 Exxon Research And Engineering Company Automatic transmission fluid having low Brookfield viscosity and high shear stability
WO2003089554A1 (en) * 2002-04-15 2003-10-30 The Lubrizol Corporation Phosphorus salts of nitrogen containing copolymers and lubricants containing the same
DE102011076364A1 (en) 2011-05-24 2012-11-29 Evonik Rohmax Additives Gmbh Lubricant composition with phosphate-functionalized polymers
WO2012159828A1 (en) 2011-05-24 2012-11-29 Evonik Rohmax Additives Gmbh Lubricant composition with phosphorus-functionalized polymers
WO2020101969A1 (en) * 2018-11-12 2020-05-22 The Lubrizol Corporation Method of lubricating an automotive or industrial gear
CN112996888A (en) * 2018-11-12 2021-06-18 路博润公司 Method for lubricating a motor vehicle or industrial gear
EP4249576A3 (en) * 2018-11-12 2023-12-06 The Lubrizol Corporation Lubricating composition for automotive or industrial gears and use thereof

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